Catalog Number UNK ATTUNE FEMORAL |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Adhesion(s) (1695); No Code Available (3191)
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Event Date 04/06/2018 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4).Initial reporter occupation: lawyer.(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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Event Description
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Medical records received ad 17 june 2019.The patient underwent a left knee revision due to instability and adhesions.The surgeon noted moderate metaphyseal bone loss after removal of the tibial tray.Unknown cement was used during the primary operation.Doi: (b)(6) 2012.Dor: (b)(6) 2018; left knee.
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Manufacturer Narrative
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Product complaint # (b)(4).Investigation summary = > the device associated with this report was not received for examination.Depuy synthes considers the investigation closed at this time.Should additional information be received, the information will be reviewed and the investigation may be re-opened as necessary.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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Search Alerts/Recalls
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